Adult solid tumours for rare diseaseGene: EPCAM
Tumor Suppressor: deletion only
Created: 5 Jul 2017, 12:19 p.m.
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes for gene: EPCAM were changed from Lynch syndrome to Colorectal cancer, hereditary nonpolyposis, type 8, OMIM:613244
5th March 2018 - promoted to version 1 after expert review and internal clinical review.
EPCAM was added to Adult solid tumours for rare disease panel. Sources: Expert list,Expert Review Green
EPCAM was created by Ellen McDonagh